Canonical Allele Identifier: CA479238387

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734108A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340306A>G , CM000674.2:g.40340306A>G	GRCh38
NC_000012.11:g.40734108A>G , CM000674.1:g.40734108A>G	GRCh37
NC_000012.10:g.39020375A>G	NCBI36
NG_011709.1:g.120296A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5961A>G MANE Select	ENSP00000298910.7:p.Ser1987=
ENST00000679360.1:c.*4870A>G	ENSP00000505368.1:n.*4870A>G
ENST00000679532.1:c.1735A>G
ENST00000680018.1:c.1406A>G	ENSP00000505347.1:n.1406A>G
ENST00000680422.1:c.1606A>G
ENST00000680425.1:c.1128A>G	ENSP00000506459.1:n.1128A>G
ENST00000680453.1:c.1418A>G
ENST00000680790.1:c.5706A>G	ENSP00000505335.1:p.Ser1902=
ENST00000681136.1:n.1945A>G
ENST00000681696.1:c.1644A>G	ENSP00000505871.1:p.Ser548=
ENST00000298910.11:c.5961A>G	ENSP00000298910.7:p.Ser1987=
ENST00000430804.5:c.3257A>G
ENST00000479187.5:n.2642A>G
NM_198578.3:c.5961A>G	NP_940980.3:p.Ser1987=
XM_005268629.2:c.5961A>G	XP_005268686.1:p.Ser1987=
XM_011537877.1:c.5961A>G	XP_011536179.1:p.Ser1987=
XM_011537878.1:c.5961A>G	XP_011536180.1:p.Ser1987=
XM_011537879.1:c.4758A>G	XP_011536181.1:p.Ser1586=
XM_005268629.4:c.5961A>G	XP_005268686.1:p.Ser1987=
XM_011537877.3:c.5961A>G	XP_011536179.1:p.Ser1987=
XM_017018787.1:c.2877A>G	XP_016874276.1:p.Ser959=
XM_017018788.2:c.2223A>G	XP_016874277.1:p.Ser741=
XM_024448833.1:c.4758A>G	XP_024304601.1:p.Ser1586=
NM_198578.4:c.5961A>G MANE Select	NP_940980.4:p.Ser1987=